A Phase 1, Placebo-controlled, Randomized, Single Ascending Dose Study and a Volunteer Infection Study to Characterize the Safety, Pharmacokinetics, and Antimalarial Activity of the Plasmodium Phosphatidylinositol 4-Kinase Inhibitor MMV390048

Author:

McCarthy James S1,Donini Cristina2,Chalon Stephan2,Woodford John1,Marquart Louise1,Collins Katharine A1,Rozenberg Felix D3,Fidock David A34,Cherkaoui-Rbati Mohammed H2,Gobeau Nathalie2,Möhrle Jörg J2ORCID

Affiliation:

1. QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia

2. Medicines for Malaria Venture, Geneva, Switzerland

3. Department of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York, USA

4. Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA

Abstract

Abstract Background MMV390048 is the first Plasmodium phosphatidylinositol 4-kinase inhibitor to reach clinical development as a new antimalarial. We aimed to characterize the safety, pharmacokinetics, and antimalarial activity of a tablet formulation of MMV390048. Methods A 2-part, phase 1 trial was conducted in healthy adults. Part 1 was a double-blind, randomized, placebo-controlled, single ascending dose study consisting of 3 cohorts (40, 80, 120 mg MMV390048). Part 2 was an open-label volunteer infection study using the Plasmodium falciparum induced blood-stage malaria model consisting of 2 cohorts (40 mg and 80 mg MMV390048). Results Twenty four subjects were enrolled in part 1 (n = 8 per cohort, randomized 3:1 MMV390048:placebo) and 15 subjects were enrolled in part 2 (40 mg [n = 7] and 80 mg [n = 8] cohorts). One subject was withdrawn from part 2 (80 mg cohort) before dosing and was not included in analyses. No serious or severe adverse events were attributed to MMV390048. The rate of parasite clearance was greater in subjects administered 80 mg compared to those administered 40 mg (clearance half-life 5.5 hours [95% confidence interval {CI}, 5.2–6.0 hours] vs 6.4 hours [95% CI, 6.0–6.9 hours]; P = .005). Pharmacokinetic/pharmacodynamic modeling estimated a minimum inhibitory concentration of 83 ng/mL and a minimal parasiticidal concentration that would achieve 90% of the maximum effect of 238 ng/mL, and predicted that a single 120-mg dose would achieve an adequate clinical and parasitological response with 92% certainty. Conclusions The safety, pharmacokinetics, and pharmacodynamics of MMV390048 support its further development as a partner drug of a single-dose combination therapy for malaria. Clinical Trials Registration NCT02783820 (part 1); NCT02783833 (part 2).

Funder

Medicines for Malaria Venture

United States Agency for International Development

Bill and Melinda Gates Foundation

Department for International Development, UK Government

Direktoratet for Utviklingssamarbeid

Irish Aid

Newcrest Mining

Wellcome Trust

National Institutes of Health

National Health and Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference20 articles.

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